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Clinical Trial Contract Coordinator - Clinical Research - Louvain-la-Neuve

Company

With 30 years of experience, our client, IDDI is seen as a valuable partner in the design, conduct and analysis of clinical trials through optimal design, innovative statistical methodology and state-of-the-art web systems.

With offices in Belgium and in Raleigh (NC, USA), IDDI has achieved very good results over the last few years.

To sustain and develop IDDI’s growth, we are looking for an experienced Clinical Trial Contract Coordinator to reinforce the Business Operation team in Belgium.

Role

Your key responsibilities will be to:

  • Coordinate proposals of projects between IDDI and the client until signature. This includes a collaboration with various external stakeholders and many departments from IDDI.
  • Analyse the received information (study protocol, Request For Proposal,…) and pro-actively collect data to facilitate the creation of the proposal with department managers, including the budget and tasks expected for the project.
  • Together with the Project Manager, act as a liaison between the client & IDDI to support the financial management of projects once the contract is signed (regular financial review and preparation of amendment).
  • Communicate timely and professionally with all stakeholders; build trust.
  • Support your colleague in the set-up and the maintenance of the ERP system once the contract is signed.
  • Assist the VP, Business Operations to detect, resolve and escalate project problems and conflicts when necessary.
  • Assist the VP, Business Operations to perform regular budget analysis for the purpose of maximizing financial and operational performance and minimizing risks.

Profile

  • Bachelor’s degree in Science, Business Administration, Accounting or business related field or equivalent experience.
  • Very good with figures and eye-for-details: you strive for a high level of accuracy.
  • Excellent knowledge of Excel.
  • Good analytical and problem solving skills.
  • Autonomous: you are able to work independently with minimal supervision.
  • Good team player.
  • Strong verbal and written communication skills.
  • Fluent English, both oral and written.
  • Experience in clinical trials and knowledge of IDDI’s areas of expertise (Randomization, Clinical Data Management and Biostatistics) is a plus.

Offer

  • A unique opportunity to work in a friendly, team-oriented and stimulating environment. Our client, IDDI, regularly organizes company-wide events such as BBQs, family-day outings, sports, and charity fundraisers, giving the chance to share time together.
  • With a low employee turnover rate, our client offers job stability and growth opportunities through on-the-job training and mentoring programs.
  • Working at IDDI will bring you an expertise that is widely recognized in our industry.
  • IDDI offers a competitive salary and benefits package including meal vouchers, hospital insurance, full reimbursement for public transport, etc. as well as flexibility for a better work-life balance (working hours, home-working opportunities, part time schedules and paid time off).

Publication date

24.09.2022

Contact person

Dumoulin

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